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Pyridin-2-yl-(3-trifluoromethyl-phenyl)-acetonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

122376-69-6

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122376-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122376-69-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122376-69:
(8*1)+(7*2)+(6*2)+(5*3)+(4*7)+(3*6)+(2*6)+(1*9)=116
116 % 10 = 6
So 122376-69-6 is a valid CAS Registry Number.

122376-69-6Relevant academic research and scientific papers

Palladium-catalyzed direct deprotonative arylation of 2-pyridylacetonitriles: Facile synthesis of alpha-aryl-2-pyridylacetonitrile

Yin, Bo,Du, Yu-Feng,Chen, Yan-Zuo,Li, Xiaohuan,Fang, Dong-Mei,Gao, Feng

, (2020)

α-Aryl-2-pyridylacetonitrile, an important chemical intermediate, was synthesized via direct deprotonative arylation of 2-pyridylacetonitrile with aryl bromides. Pd(OAc)2/NixantPhos-based catalysis system promoted this arylation reaction to furnish divers

Structure-activity relationship and cardiac safety of 2-aryl-2-(pyridin-2-yl)acetamides as a new class of broad-spectrum anticonvulsants derived from Disopyramide

?tengl, Milan,Chodkowski, Andrzej,Dawidowski, Maciej,El Harchi, Aziza,Hancox, Jules C.,Jarkovska, Dagmar,Konopelski, Piotr,Król, Marek,Mistrova, Eliska,Podsadni, Piotr,Popowicz, Grzegorz M.,Sviglerova, Jitka,Szuberski, Piotr,Szulczyk, Bart?omiej,Tur?o, Jadwiga,Ufnal, Marcin,Wróbel, Martyna Zofia,Zhang, Yihong

, (2020/03/17)

A series of 2-aryl-2-(pyridin-2-yl)acetamides were synthesized and screened for their anticonvulsant activity in animal models of epilepsy. The compounds were broadly active in the ‘classical’ maximal electroshock seizure (MES) and subcutaneous Metrazol (scMET) tests as well as in the 6 Hz and kindling models of pharmacoresistant seizures. Furthermore, the compounds showed good therapeutic indices between anticonvulsant activity and motor impairment. Structure-activity relationship (SAR) trends clearly showed the highest activity resides in unsubstituted phenyl derivatives or compounds having ortho- and meta- substituents on the phenyl ring. The 2-aryl-2-(pyridin-2-yl)acetamides were derived by redesign of the cardiotoxic sodium channel blocker Disopyramide (DISO). Our results show that the compounds preserve the capability of the parent compound to inhibit voltage gated sodium currents in patch-clamp experiments; however, in contrast to DISO, a representative compound from the series 1 displays high levels of cardiac safety in a panel of in vitro and in vivo experiments.

Synthesis of Primary ω-Phenyl-ω-pyridylalkylamines

Buschauer, Armin

, p. 165 - 171 (2007/10/02)

Phthalimidoalkylation of phenylpyridylacetonitriles followed by acidic or basic hydrolysis and decarboxylation is a convenient method for the preparation of pheniramine-like primary amines.Substituted dihydropyrrolamines were isolated as intermediates in the synthesis of the corresponding propylamines.Alternatively, 3,3-diarylpropylamines were prepared via Horner-Emmons reaction of pertinent ketones with diethyl cyanomethanephosphonate followed by reduction with complex hydrides.

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